GMP Compliance Specialist

8 hours ago


Hillerød, Hillerød Kommune, Denmark Novo Nordisk AS Full time
About the Role

We are seeking a highly motivated and organized professional to support our department in maintaining compliance with current Good Manufacturing Practice (cGMP) regulations.

Key Responsibilities
  • Collaborate with the team to identify continuous improvement opportunities and implement process enhancements.
  • Drive transparency initiatives for key quality indicators, including collecting data, preparing reports, and following up on action items.
  • Analyze trends and provide recommendations for process improvements.
  • Serve as the primary point of contact for GMP-related matters and coordinate inspections and audits.
Requirements
  • Bachelor's degree in a relevant field, such as pharmacy, chemical engineering, or biology.
  • Minimum 2 years of experience in the pharmaceutical or medical device industry.
  • Strong understanding of GMP regulations and compliance.
  • Excellent communication and coordination skills.
About the Department

The AMSAT QC department is responsible for analyzing products and providing high-quality results. We have a strong focus on digitalization and automation, and we work closely with cross-functional teams to drive innovation.

Working at Novo Nordisk A/S

We strive to create an inclusive and dynamic work environment where employees can grow professionally and personally. As part of our team, you will be challenged to think creatively and contribute to improving the lives of patients worldwide.



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